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pfm medical, inc.Principal Clinical Data Scientist
pfm medical, inc. seeks a remote Principal Clinical Data Scientist to act as the functional lead for clinical science analytics and insights operations across assigned projects.…
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About This Role
pfm medical, inc. seeks a remote Principal Clinical Data Scientist to act as the functional lead for clinical science analytics and insights operations across assigned projects. This professional will manage study processes spanning from initial startup all the way through database lock. The role involves guiding cross-functional teams in scientific data review, overseeing medical monitor reviews, helping develop electronic case report forms, and driving data cleaning initiatives. Ideal candidates will…
Job Description
pfm medical, inc. seeks a remote Principal Clinical Data Scientist to act as the functional lead for clinical science analytics and insights operations across assigned projects. This professional will manage study processes spanning from initial startup all the way through database lock. The role involves guiding cross-functional teams in scientific data review, overseeing medical monitor reviews, helping develop electronic case report forms, and driving data cleaning initiatives. Ideal candidates will combine deep oncology knowledge with strong organizational abilities to independently direct clinical data review functions, monitor study risks, and collaborate effectively across global project groups. This position offers the opportunity to work remotely while applying advanced clinical expertise to trial data visualization outputs and safety monitoring.
Responsibilities
- Serve as the functional lead implementing clinical science analytics and insights services on designated project teams.
- Act as a project team resource for scientific data capture, cleaning, and review activities.
- Manage the overall internal data cleaning process to support interim and final study deliverables.
- Oversee medical monitor review of subject data and provide scientific operational protocol reviews.
- Collaborate with data management on electronic case report form specifications, edit checks, and user acceptance testing.
- Conduct aggregate and holistic scientific clinical-sense data review using programmed outputs, listings, and graphs.
- Issue and resolve queries within electronic data capture systems while providing routine status updates on findings.
- Develop, maintain, and oversee project-related plans, trackers, guidelines, and electronic trial master file documentation.
Requirements
- Minimum of 8 years of clinical research experience or proven competencies for the position.
- Minimum of 1 year of leadership experience.
- Proficiency in medical terminology and familiarity with electronic data capture systems.
- Strong working knowledge of Microsoft Office products including Outlook, Word, Excel, and PowerPoint.
- Professional written and verbal communication skills in English with solid interpersonal capabilities.
- Legal authorization to work in the employment country without requiring employer sponsorship.
- Ability to occasionally travel domestically and internationally with overnight stays.
Qualifications
- Bachelor's degree or equivalent combination of education and experience in a science or health-related discipline.
- Medical-related degree such as RN, OCN, RPH, or PharmD.
- Prior experience with database building or on-site monitoring.
- Experience utilizing data visualization software like JReview.
- Previous professional exposure to solid and liquid tumors.
- Background working on phase I, II, and III studies as well as global clinical trials.
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, the posting indicates that the employment type is remote and the role allows for working remotely.
What is the salary for this role?
The job posting does not specify the salary.
What level of experience is required?
Candidates must have a minimum of 8 years of clinical research experience or proven competencies, alongside at least 1 year of leadership experience.
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